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TargetIntegrase
LigandBDBM50042007
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1443856 (CHEMBL3373530)
IC50 4.0±n/a nM
Citation Naidu, BNSorenson, MEPatel, MUeda, YBanville, JBeaulieu, FBollini, SDicker, IBHigley, HLin, ZPajor, LParker, DDTerry, BJZheng, MMartel, AMeanwell, NAKrystal, MWalker, MA Synthesis and evaluation of C2-carbon-linked heterocyclic-5-hydroxy-6-oxo-dihydropyrimidine-4-carboxamides as HIV-1 integrase inhibitors. Bioorg Med Chem Lett25:717-20 (2015) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Integrase
Name:Integrase
Synonyms:pol
Type:PROTEIN
Mol. Mass.:32203.43
Organism:Human immunodeficiency virus 1
Description:ChEMBL_106649
Residue:288
Sequence:
FLDGIDKAQEEHEKYHSNWRAMASDFNLPPVVAKEIVASCDKCQLKGEAMHGQVDCSPGI
WQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAGRWPVKTVHTDNGSN
FTSTTVKAACWWAGIKQEFGIPYNPQSQGVIESMNKELKKIIGQVRDQAEHLKTAVQMAV
FIHNFKRKGGIGGYSAGERIVDIIATDIQTKELQKQITKIQNFRVYYRDSRDPVWKGPAK
LLWKGEGAVVIQDNSDIKVVPRRKAKIIRDYGKQMAGDDCVASRQDED
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50042007
n/a
NameBDBM50042007
Synonyms:CHEMBL3360111
TypeSmall organic molecule
Emp. Form.C17H18FN3O4
Mol. Mass.347.3409
SMILESCn1c(nc(C(=O)NCc2ccc(F)cc2)c(O)c1=O)C1CCOC1
Structure
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